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FDA 510(k)

EFTEKHAR ACETABULAR STANDOFF

K-Number: K811201 · 1981-05-21

ApplicantZimmer, Inc.
Decision Date1981-05-21
Product Code
DecisionSubstantially Equivalent

Device Summary

EFTEKHAR ACETABULAR STANDOFF is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1981-05-21 under 510(k) number K811201. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EFTEKHAR ACETABULAR STANDOFF?

EFTEKHAR ACETABULAR STANDOFF is a medical device that received FDA 510(k) clearance on 1981-05-21. The listed applicant is Zimmer, Inc.. The 510(k) number is K811201.

When did EFTEKHAR ACETABULAR STANDOFF receive FDA 510(k) clearance?

EFTEKHAR ACETABULAR STANDOFF received FDA 510(k) clearance on 1981-05-21, under 510(k) number K811201.

Who is the listed applicant for EFTEKHAR ACETABULAR STANDOFF?

The FDA 510(k) record lists Zimmer, Inc. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Zimmer, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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